玉米裸芽病毒1型感染玉米玉米卵巢细胞系的转录动力学。

IF 3.6 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of General Virology Pub Date : 2025-01-01 DOI:10.1099/jgv.0.002066
Jirka Manuel Petersen, Astrid Bryon, Annie Bézier, Jean-Michel Drezen, Monique M van Oers
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引用次数: 0

摘要

裸病毒(裸病毒科)是一种感染各种昆虫和甲壳类动物的双链DNA病毒。其中,Heliothis zea裸病毒1 (HzNV-1)是鳞翅目裸病毒引起性病理的罕见病例。关于HzNV-1或其他裸病毒分子病理动力学的研究很少。因此,本研究旨在提供HzNV-1在玉米Helicoverpa zea卵巢来源细胞系(HZ-AM1)感染早期(感染后3、6和9小时)和晚期(感染后12和24小时)的转录组学特征。从病毒和模拟感染的细胞中提取总RNA,并进行RNA-seq分析以检查病毒和宿主的转录动力学。采用层次聚类方法对病毒基因进行分类,采用差异基因表达分析方法确定受感染显著影响的宿主基因。分层聚类将154个HzNV-1基因分为4个时间阶段,早期主要涉及转录和复制基因,后期主要涉及病毒粒子组装基因。此外,在早期表达基因的上游区域发现了一个新的病毒启动子基序。宿主基因分析显示,热休克蛋白基因显著上调,组蛋白基因显著下调。病毒基因表达时间模式的鉴定增强了对裸病毒病理的分子理解,而鉴定的差异表达宿主基因突出了被HzNV-1感染劫持最多的关键途径。
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Transcriptional dynamics during Heliothis zea nudivirus 1 infection in an ovarian cell line from Helicoverpa zea.

Nudiviruses (family Nudiviridae) are double-stranded DNA viruses that infect various insects and crustaceans. Among them, Heliothis zea nudivirus 1 (HzNV-1) represents the rare case of a lepidopteran nudivirus inducing a sexual pathology. Studies about molecular pathological dynamics of HzNV-1 or other nudiviruses are scarce. Hence, this study aims to provide a transcriptomic profile of HzNV-1 in an ovary-derived cell line of Helicoverpa zea (HZ-AM1), during early (3, 6 and 9 h post-infection) and advanced (12 and 24 h post-infection) stages of infection. Total RNA was extracted from both virus- and mock-infected cells, and RNA-seq analysis was performed to examine both virus and host transcriptional dynamics. Hierarchical clustering was used to categorize viral genes, while differential gene expression analysis was utilized to pinpoint host genes that are significantly affected by the infection. Hierarchical clustering classified the 154 HzNV-1 genes into four temporal phases, with early phases mainly involving transcription and replication genes and later phases including genes for virion assembly. In addition, a novel viral promoter motif was identified in the upstream region of early-expressed genes. Host gene analysis revealed significant upregulation of heat shock protein genes and downregulation of histone genes. The identification of temporal patterns in viral gene expression enhances the molecular understanding of nudivirus pathology, while the identified differentially expressed host genes highlight the key pathways most hijacked by HzNV-1 infection.

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来源期刊
Journal of General Virology
Journal of General Virology 医学-病毒学
CiteScore
7.70
自引率
2.60%
发文量
91
审稿时长
3 months
期刊介绍: JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.
期刊最新文献
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